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About the vacancy
ExpertMaster’s Degree (WO) Permanent Full-time 9052 Ghent, Belgium
About Your Next Job The QS Associate QRM & Excellence is responsible for supporting the continuous improvement within the quality systems department of CAR-T Belgium (Ghent and Beerse). This includes the execution of lean/six sigma projects and maintaining & improving the quality risk management (QRM) framework.
About Your Skills and Experience Requirements and qualifications:
Master’s degree in a scientific/technical field and 2–3 years of experience in a GMP environment.
Solid knowledge of pharmaceutical regulations and GMP standards.
Familiarity with core QS processes (CAPA, Change Control, Deviations, Document Management).
Exposure to Lean/Six Sigma methodologies and proficiency in data analysis tools (Excel, Minitab).
Understanding of risk management standards (ICH Q9, ISO 31000) and experience with Health Authority inspections.
Strong analytical, decision-making, and organizational skills; able to manage multiple tasks independently.
Excellent communication skills for effective interaction with internal and external stakeholders.
Where Molecules Meet Opportunities Hybrid Work
You are eligible to work in EU We only accept applicants who are eligible to work in the EU.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
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About Your Next Job The QS Associate QRM & Excellence is responsible for supporting the continuous improvement within the quality systems department of CAR-T Belgium (Ghent and Beerse). This includes the execution of lean/six sigma projects and maintaining & improving the quality risk management (QRM) framework.
About Your Skills and Experience Requirements and qualifications:
Master’s degree in a scientific/technical field and 2–3 years of experience in a GMP environment.
Solid knowledge of pharmaceutical regulations and GMP standards.
Familiarity with core QS processes (CAPA, Change Control, Deviations, Document Management).
Exposure to Lean/Six Sigma methodologies and proficiency in data analysis tools (Excel, Minitab).
Understanding of risk management standards (ICH Q9, ISO 31000) and experience with Health Authority inspections.
Strong analytical, decision-making, and organizational skills; able to manage multiple tasks independently.
Excellent communication skills for effective interaction with internal and external stakeholders.
Where Molecules Meet Opportunities Hybrid Work
You are eligible to work in EU We only accept applicants who are eligible to work in the EU.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
#J-18808-Ljbffr